Chain415: Congenital Slow Channel Myasthenic Syndrome

This is a rare disease.

Example use A

Rare disease screening of newborns or adults thinking of having children. Could also be used as part of a comprehensive analysis of a person's genes.

Developer

Dr. Colby

Genetic info

GenesGenetic variants
CHRNB1chr17:7357648,chr17:7357660
CHRNEchr17:4804366,chr17:4805305,chr17:4804140
CHRNA1chr2:175618970

Qualitative

Type

text

Possible responses

Carrier, Possibly Affected, Not Detected, insufficient data, error